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21.
瘿绵蚜科系统发育研究(同翅目:蚜总科)   总被引:1,自引:0,他引:1  
张广学  陈小琳 《昆虫学报》1999,42(2):176-183
采用支序分析的方法对瘿绵蚜科的系统发育进行了探讨。研究结果表明,传统的倍蚜族Schlechtendalini、五节根蚜族Fordini和瘿绵蚜族Pemphigini 是单系群,传统的 卷叶绵蚜族Prociphilini 和四脉绵蚜族Tetraneurini是并系群。在瘿绵蚜科的三个亚科中,瘿绵蚜亚科与五节根蚜亚科亲缘关系比与绵蚜亚科更近。另外,根据支序分析结果,建议将丽绵蚜属Formosaphis从瘿绵蚜亚科移入五节根蚜亚科中。  相似文献   
22.
辣椒蚜虫种类的调查   总被引:3,自引:0,他引:3  
蚜虫属同翅目蚜虫总科,是重要的作物害虫。调查海南辣椒植株的蚜虫种类,采集蚜虫标本。将上述活体蚜虫分别接种在室内盆栽辣椒植株上饲养、繁殖,并观察记录各龄期蚜虫的形态特征。经室内观察测定,鉴定出三种蚜虫:棉蚜[Aphis gossypii(Glover)]、桃蚜[Myzus persicae(Sulzer)]和萝卜蚜[Lipaphis erysimi(Kaltenbach)]。  相似文献   
23.
甘肃省蚜虫类物种多样性研究   总被引:13,自引:5,他引:8  
在已有标本采集记录和资料的基础上,从分类阶元、寄主植物、寄生部位、动物地理区系的角度探讨了甘肃省蚜虫类的物种多样性。结果表明甘肃省蚜虫种类丰富,已知9科90属220种;分布在华北区、蒙新区、青藏区、华中区和西南区,其中华北区、蒙新区和青藏区的种类最为丰富,因此甘肃省蚜虫区系以古北界成分为主;寄主植物种类繁多,已知有46科111属;寄生部位多样化,以叶片和茎为主要为害部位。另外就甘肃省所处地理位置的特殊性,初步讨论了在不同地理区划交界处物种生物多样性所受的影响。  相似文献   
24.
中国蚜虫类昆虫物种多样性与分布特点(半翅目,蚜总科)   总被引:3,自引:0,他引:3  
研究了蚜虫类昆虫在中国的物种多样性、区系成分和分布特点.基于多年的标本采集记录和已发表文献,建立了中国蚜虫物种数据库和中国蚜虫地理分布数据库.应用GIS的空间分析功能对中国蚜虫的地理分布和分布密度进行了分析.结果表明中国记录蚜虫类昆虫268属1 099种/亚种,其中特有种518种,占中国蚜虫物种总数的47.1%.中国蚜虫的区系成分十分复杂,主要分为9种类型,其中以典型古北种、典型东洋种、跨古北界和东洋界分布的物种为主,同时与新北界、澳洲界的关系也较为密切.在自然地理区划上,蚜虫在中国东部地区的分布多于西部地区,中部地区多于南北两端.基于物种多样性和分布密度,确定了蚜虫在中国的5个多样性中心,即甘南山地、横断山区、天山山地、东部平原和台湾岛.  相似文献   
25.
云杉蚜虫-天敌-杀虫剂相互作用控制模型的动态特性   总被引:2,自引:0,他引:2  
使用微分方程与控制理论研究了使用杀虫剂对一类云杉蚜虫与其天敌相互作用模型的动态特性的影响.其中包括云杉蚜虫-天敌-杀虫剂相互作用控制模型正平衡点存在个数及正平衡点的稳定性与杀虫剂使用量的关系.研究结果表明:适当地使用杀虫剂可以在天敌数量不足的情况下控制害虫爆发的事件.  相似文献   
26.
小麦蚜虫是世界范围内小麦生产中一类重要害虫。针对麦蚜世代历期短、繁殖力强,具有趋光、趋化及迁飞等生物学及行为习性;在田间多呈聚集分布,且麦蚜易受寄主植物抗性、天敌、气象因素及农田生态条件等生物与非生物因素影响等发生为害特点,本文阐述了我国小麦蚜虫田间调查、监测技术及防治策略,以期为我国小麦蚜虫综合防控提供基础科学支撑。  相似文献   
27.
以黄粉虫为基础营养组分配制的人工饲料,能満足龟纹瓢虫幼虫和成虫生长发育需要,筛选的配方具有材料来源广泛、成本低等优点,但连续喂饲人工饲料3代,会导致幼虫历期、蛹历期延长,羽化率、成虫获得率、孵化率降低等现象,生产上应通过野化等措施加以解决。在野外释放人工饲料扩繁的龟纹瓢虫成虫以瓢蚜比1:1防治园林蚜虫,取得了良好效果,可以不用打药而能有效地控制蚜害。  相似文献   
28.
Abstract Aphids may harbor a wide variety of facultative bacterial endosymbionts. These symbionts are transmitted maternally with high fidelity and they show horizontal trans-mission as well, albeit at rates too low to enable infectious spread. Such symbionts need to provide a net fitness benefit to their hosts to persist and spread. Several symbionts haveachieved this by evolving the ability to protect their hosts against parasitoids. Reviewing empirical work and some models, I explore the evolutionary ecology of symbiont-conferredresistance to parasitoids in order to understand how defensive symbiont frequencies are maintained at the intermediate levels observed in aphid populations. I further show thatdefensive symbionts alter the reciprocal selection between aphids and parasitoids by augmenting the heritable variation for resistance, by increasing the genetic specificity of thehost-parasitoid interaction, and by inducing environment-dependent trade-offs. These effects are conducive to very dynamic, symbiont-mediated coevolution that is driven by frequency-dependent selection. Finally I argue that defensive symbionts represent a problem for biological control of pest aphids, and I propose to mitigate this problem byexploiting the parasitoids' demonstrated ability to rapidly evolve counteradaptations to symbiont-conferred resistance.  相似文献   
29.
The soybean aphid Aphis glycines Matsumura (Hemiptera: Aphididae) is an important pest of soybean in China. To monitor and manage this pest effectively it is neces-sary to understand its population dynamics and demographics, as well as the physiological responses of soybean plants to its feeding. In this study, using field surveying and suction-trap monitoring, we investigated the population dynamics of the soybean aphid in Xiuyan County, Liaoning Province in northeastern China during 2009-2012. The results indicatedthat the population dynamics of the soybean aphid followed a unimodal curve distribution, with the insect generally colonizing soybean fields from the middle of June to early Julyand the population reaching a peak between early July and early August. On the whole, soybean aphids occurred in suction-traps at least 2 weeks earlier than they were foundin field surveys. A total of 72 alates were collected by suction-trapping over the 4 years, with the earliest alate captures occurring on 28 May in 2009, 2011, 2012 and 4 June in 2010. The life table parameters clearly showed that this aphid had a short doubling time (4.73 ± 0.21 days), and 7.36± 0.98 nymphs were produced by a soybean aphid adult during its lifetime (13.57 ± 0.30 days). Finally, biochemical assays indicated that the amount of malondialdehyde and the activities of four defense-related enzymes in soybean leavessignificantly changed between 0 day and 7 days of aphid infestation. Polyphenol oxidase (PPO) and catalase (CAT) activities increased more dramatically after 1 day of aphid feed-ing. In addition, significantly higher levels of superoxide dismutase and CAT were found after aphid feeding for 7 days, whereas there was no significant change in the activitiesof peroxidase and PPO. Consequently, this study will be beneficial in determining the seasonal occurrence of the soybean aphid and selecting insect-resistant soybean varieties,and thus in developing a theoretical framework for appropriate management strategies.  相似文献   
30.
Aphids (Hemiptera: Aphididae) are a group of phloemfeeding insects numbering more than 5 000 extant species(Favret, 2014a). Most species have complex life cycles that include both asexual (viviparous parthenogenesis)and sexual reproduction. They display a high degree of intraspecific polyphenism with multiple phenotypes froman identical genotype, and they have specialized associations with their host plants (Blackman & Eastop, 2000).Some aphid species are gall-makers and even have evolved sociality with division of labor (Aoki, 1977; Stern &Foster, 1996). Many aphid species are agricultural and forestry pests. They incur damage to plants and carryvector plant viruses (Blackman & Eastop, 2000). Due to their fascinating biological character and economic importance, aphids have long been popular animals for research in basic and applied biology, and are becominguseful research models for studying important questions in ecology and evolution, especially in the genomic era(Brisson & Stem, 2006; Huang & Qiao, 2006; Srinivasan & Brisson, 2012).  相似文献   
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